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455999

CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324377
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccccc2)cc1
Reaction #324378
Compound 11a
Выход 75.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324379
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2/C=C/c2ccccc2)cc1
Reaction #324380
Compound 11b
Выход 69.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324381
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
C=C(c1ccccc1)c1nc(-c2ccc(O[Si](C)(C)C(C)(C)C)cc2)cnc1NC(=O)Cc1ccc(O[Si](C)(C)C(C)(C)C)cc1
Reaction #324382
Compound 11c
Выход 33.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324383
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cccc3ccccc23)cc1
Reaction #324384
Compound 11d
Выход 55.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324385
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccc3ccccc3c2)cc1
Reaction #324386
Compound 11e
Выход 58.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324387
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cccs2)cc1
Reaction #324388
Compound 11f
Выход 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324389
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccsc2)cc1
Reaction #324390
Compound 11g
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324391
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2cc3ccccc3s2)cc1
Reaction #324392
Compound 11h
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324393
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2csc3ccccc23)cc1
Reaction #324394
Compound 11i
Выход 63.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
Reaction #324395
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Nc2ncc(-c3ccc(O[Si](C)(C)C(C)(C)C)cc3)nc2-c2ccc(O[Si](C)(C)C(C)(C)C)cc2)cc1
Reaction #324396
Compound 11j
Выход 81.1%DOI: 10.6084/m9.figshare.5104873.v1
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